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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1169808생성일: 2026년 10월 27일

Diisopropylethylamine → 2-[1-(2-Tert-butyl-6-chloro-5-methyl-pyrimidin-4-yl)-piperidin-4-yl]-[1,8]naphthyridine

https://huagongshe.com/reaction/1169808

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1,8-NaphthyridineHCID 136069—
반응물Sodium BicarbonateHCID 516892—
반응물2-Tert-butyl-4,6-dichloro-5-methylpyrimidineHCID 824660—
반응물2-(Piperidin-4-YL)-1,8-naphthyridineHCID 66640919—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
용매DimethylacetamideHCID 31374—
생성물2-[1-(2-Tert-butyl-6-chloro-5-methyl-pyrimidin-4-yl)-piperidin-4-yl]-[1,8]naphthyridineHCID 8661892865.4%

반응 조건

온도100 °C

반응 단계

20 ml of dimethylacetamide and 5 ml (17.8 mmoles) of diisopropylethylamine are added into a single-necked flask containing 1.5 g (6.84 mmoles) of 2-tert-butyl-4,6-dichloro-5-methyl-pyrimidine and 1.46 g (6.84 mmoles) of 2-piperidin-4-yl-[1,8]naphthyridine. This mixture is heated at 100° C. overnight. The next day 0.2 equivalent of naphthyridine is added and the mixture is heated for another 6 hours. The reaction mixture is returned to ambient temperature before concentrating to dryness. The residue obtained is taken up in a mixture of water, ethyl acetate and a saturated solution of sodium bicarbonate. The organic phase is separated and the aqueous phase reextracted with ethyl acetate. The collected organic phases are dried over magnesium sulphate then the solvent is evaporated off under reduced pressure (2 kPa). The residue is chromatographed on silica gel eluting with a gradient of heptane-ethyl acetate (70-30) to heptane-ethyl acetate (50-50). 1.77 g of expected product is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07825119B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-6bae5d17e4d74606bb865bc86c3064c9
출처 메모uspto-grants-2010_11